HK1020884A1 - Purine inhibitors of cyclin dependent kinase 2 andikb-alpha. - Google Patents

Purine inhibitors of cyclin dependent kinase 2 andikb-alpha.

Info

Publication number
HK1020884A1
HK1020884A1 HK99106194A HK99106194A HK1020884A1 HK 1020884 A1 HK1020884 A1 HK 1020884A1 HK 99106194 A HK99106194 A HK 99106194A HK 99106194 A HK99106194 A HK 99106194A HK 1020884 A1 HK1020884 A1 HK 1020884A1
Authority
HK
Hong Kong
Prior art keywords
alkyl
substituted
cycloalkyl
benzylamino
cycloheteroalkyl
Prior art date
Application number
HK99106194A
Inventor
Robert T Lum
Cheri Lynn Blum
Richard Mackman
Michael M Wick
Steven R Schow
Original Assignee
Cv Therapeutics Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Cv Therapeutics Inc filed Critical Cv Therapeutics Inc
Publication of HK1020884A1 publication Critical patent/HK1020884A1/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52—Purines, e.g. adenine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10—Antimycotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/40—Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Cardiology (AREA)
  • Biomedical Technology (AREA)
  • Endocrinology (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Emergency Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A 2,6,9-trisubstituted purine composition having the following formula: <IMAGE> where X is a amino, oxo, thio, of sulfone moiety, R1 is a lower alkyl, substituted lower alkyl, cycloalkyl, substituted cycloalkyl, cycloheteroalkyl, substituted cycloheteroalkyl, aryl, substituted aryl, heterocycle, hetaryl, substituted hetaryl, aralkyl, heteroaralkyl, heteroalkyl, alkyl alkenyl, alkyl alkynyl, alkyl cycloalkyl, or alkyl cycloheteroalkyl, each having from 1 to 20 carbon atoms; R2 is hydrogen, lower alkyl, substituted lower alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, heterocycle, hetaryl, substituted hetaryl, aralkyl, heteroaralkyl, heteroalkyl, alkyl alkenyl, alkyl alkynyl, alkyl cycloalkyl, or alkyl cycloheteroalkyl; and R3 is halogen, hydroxyl, thio, alkoxy, alkylthio, lower alkyl, -NR4R5 or a component having the formula: <IMAGE> wherein when R3 is 2-hydroxyethylamino and R2 is methyl, R1-X is not amino, 3-methyl-2-butenylamino, benzylamino, or m-hydroxybenzyl-amino, when R3 is 2-hydroxyethylamino and R2 is isopropyl, R1-X is not benzylamino, m-hydroxybenzylamino, or 3-methylbutylamino, when R3 is 2-hydroxyethylamino and R2 is 2-hydroxyethyl, R1-X is not benzylamino and when R3 is selected from the group consisting of 2-propanol-2-methylamino and 2-dimethylaminoethylamino and R2 is methyl, then R1-X is not benzylamino.
HK99106194A 1996-08-02 1999-12-30 Purine inhibitors of cyclin dependent kinase 2 andikb-alpha. HK1020884A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/692,012 US5866702A (en) 1996-08-02 1996-08-02 Purine inhibitors of cyclin dependent kinase 2
PCT/US1997/013386 WO1998005335A1 (en) 1996-08-02 1997-08-01 PURINE INHIBITORS OF CYCLIN DEPENDENT KINASE 2 AND IλB-$g(a)

Publications (1)

Publication Number Publication Date
HK1020884A1 true HK1020884A1 (en) 2000-05-26

Family

ID=24778922

Family Applications (1)

Application Number Title Priority Date Filing Date
HK99106194A HK1020884A1 (en) 1996-08-02 1999-12-30 Purine inhibitors of cyclin dependent kinase 2 andikb-alpha.

Country Status (26)

Country Link
US (1) US5866702A (en)
EP (1) EP1021186B1 (en)
JP (1) JP2000515550A (en)
KR (1) KR100403336B1 (en)
CN (1) CN1161356C (en)
AT (1) ATE298572T1 (en)
AU (1) AU731778B2 (en)
BR (1) BR9710801A (en)
CA (1) CA2262454C (en)
CZ (1) CZ299381B6 (en)
DE (1) DE69733674T2 (en)
DK (1) DK1021186T3 (en)
ES (1) ES2242981T3 (en)
GE (1) GEP20022786B (en)
HK (1) HK1020884A1 (en)
HU (1) HUP9902414A3 (en)
IL (1) IL128323A (en)
NO (1) NO323775B1 (en)
NZ (1) NZ334061A (en)
PL (1) PL189775B1 (en)
PT (1) PT1021186E (en)
RU (1) RU2220968C2 (en)
SI (1) SI1021186T1 (en)
TR (1) TR199900683T2 (en)
UA (1) UA71890C2 (en)
WO (1) WO1998005335A1 (en)

Families Citing this family (145)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4004066B2 (en) * 1995-11-01 2007-11-07 ノバルティス アクチエンゲゼルシャフト Purine derivatives and process for producing the same
FR2741881B1 (en) * 1995-12-01 1999-07-30 Centre Nat Rech Scient NOVEL PURINE DERIVATIVES HAVING IN PARTICULAR ANTI-PROLIFERATIVE PRORIETES AND THEIR BIOLOGICAL APPLICATIONS
US6790958B2 (en) * 1996-08-02 2004-09-14 Robert T. Lum Purine inhibitors of cyclin dependent kinase 2 & IKBA
WO1998016528A1 (en) 1996-10-11 1998-04-23 Chiron Corporation Purine inhibitors of glycogen synthase kinase 3 (gsk3)
DE19653646A1 (en) * 1996-12-20 1998-06-25 Hoechst Ag Substituted purine derivatives, processes for their preparation, agents containing them and their use
AU744986B2 (en) * 1997-07-12 2002-03-07 Cancer Research Technology Limited Cyclin dependent kinase inhibiting purine derivatives
US6573044B1 (en) * 1997-08-07 2003-06-03 The Regents Of The University Of California Methods of using chemical libraries to search for new kinase inhibitors
CA2297967A1 (en) 1997-08-07 1999-02-18 The Regents Of The University Of California Purine inhibitor of protein kinases, g proteins and polymerases
EP1418244A1 (en) * 1997-12-19 2004-05-12 Affymetrix, Inc. Exploiting genomics in the search for new drugs
DE69822206T2 (en) 1997-12-19 2005-02-17 Affymetrix, Inc., Santa Clara KNOWLEDGE OF GENOME RESEARCH FOR THE SEARCH FOR NOVEL ACTIVE SUBSTANCES
US6413974B1 (en) 1998-02-26 2002-07-02 Aventis Pharmaceuticals Inc. 6,9,-disubstituted 2-[trans-(4-aminocyclohexyl) amino] purines
US6642231B2 (en) * 1998-02-26 2003-11-04 Aventis Pharmaceuticals Inc. 6,9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines
US6479487B1 (en) * 1998-02-26 2002-11-12 Aventis Pharmaceuticals Inc. 6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines
US6703395B2 (en) 1998-03-04 2004-03-09 Institute Of Experimental Botany Of The Academy Of Sciences Of The Czech Republic Cyclin dependent kinase inhibitor
US6221873B1 (en) 1998-03-04 2001-04-24 Institute Of Experimental Botany Of The Academy Of Sciences Of The Czech Republic Cyclin dependent kinase inhibitor
GB9806739D0 (en) * 1998-03-28 1998-05-27 Univ Newcastle Ventures Ltd Cyclin dependent kinase inhibitors
DE69930120T2 (en) * 1998-06-16 2006-11-02 The Government of the United States of America, as represented by the Secretary National Institute of Health, Office of Technology Transfer ANNEXED AZEPINONE AS INHIBITORS CYCLIN-DEPENDENT KINASES
US6559152B2 (en) 1998-10-13 2003-05-06 Dupont Pharmaceuticals Company 6-substituted pyrazolo[3,4-d]pyrimidin-4-ones useful as cyclin dependent kinase inhibitors
US6531477B1 (en) 1998-10-13 2003-03-11 Dupont Pharmaceuticals Company 6-substituted pyrazolo [3,4-d] pyrimidin-4-ones useful as cyclin dependent kinase inhibitors
KR100377138B1 (en) * 1998-11-10 2003-06-12 주식회사 엘지생명과학 Cyclin's Zonkinase Inhibitor with Purine Structure, Methods for Making the Same, and Anticancer Compositions Containing the Same
CZ27399A3 (en) * 1999-01-26 2000-08-16 Ústav Experimentální Botaniky Av Čr Substituted nitrogen heterocyclic derivatives process of their preparation, the derivatives employed as medicaments, pharmaceutical composition and a compound pharmaceutical preparation in which these derivatives are comprised as well as use of these derivatives for preparing medicaments
GEP20033092B (en) * 1999-02-01 2003-10-27 Cv Therapeutics Inc Us Purine Inhibitors of Cyclin Dependent Kinase 2 and Ik-Aa
AU2004200192B2 (en) * 1999-02-01 2006-11-16 Gilead Palo Alto, Inc. Purine inhibitors of cyclin dependent kinase 2 and 1k-Aa
KR100368515B1 (en) * 1999-02-03 2003-01-24 주식회사 엘지생명과학 Cyclin dependent kinase inhibitor and method of preparing the same
KR20000055080A (en) * 1999-02-03 2000-09-05 성재갑 Cyclin dependent kinase inhibitor and method of preparing the same
GB9903762D0 (en) 1999-02-18 1999-04-14 Novartis Ag Organic compounds
US6624171B1 (en) 1999-03-04 2003-09-23 Smithkline Beecham Corporation Substituted aza-oxindole derivatives
GB9904933D0 (en) 1999-03-04 1999-04-28 Glaxo Group Ltd Compounds
US6627633B2 (en) 1999-03-17 2003-09-30 Albany Molecular Research, Inc. 6-substituted biaryl purine derivatives as potent cyclin/CDK inhibitors and antiproliferative agents
US6969720B2 (en) 1999-03-17 2005-11-29 Amr Technology, Inc. Biaryl substituted purine derivatives as potent antiproliferative agents
FR2793794B1 (en) * 1999-05-21 2001-07-27 Hoechst Marion Roussel Inc NOVEL PURINE DERIVATIVES, THEIR PREPARATION PROCESS, THEIR APPLICATION AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND NEW USE
EP1194425B1 (en) 1999-06-23 2005-08-10 Aventis Pharma Deutschland GmbH Substituted benzimidazole
GB9918035D0 (en) * 1999-07-30 1999-09-29 Novartis Ag Organic compounds
US6420384B2 (en) * 1999-12-17 2002-07-16 Ariad Pharmaceuticals, Inc. Proton pump inhibitors
ATE322494T1 (en) * 2000-01-07 2006-04-15 Universitaire Instelling Antwe PURINE DERIVATIVES, THEIR PRODUCTION AND USE
KR20010077073A (en) * 2000-01-31 2001-08-17 박호군 C-2,6,9 substituted isopropylpurine derivatives and a preparation thereof
GB0016877D0 (en) * 2000-07-11 2000-08-30 Astrazeneca Ab Chemical compounds
US6861524B2 (en) 2000-10-31 2005-03-01 Aventis Pharmaceuticals Inc. Acyl and sulfonyl derivatives of 6,9-disubstituted 2-(trans-1,4-diaminocyclohexyl)-purines and their use as antiproliferative agents
FR2818278B1 (en) * 2000-12-20 2003-02-28 Sod Conseils Rech Applic INHIBITORS OF CYCLIN DEPENDENT KINASES (CDK) AND GLYCOGEN SYNTHASE KINASE-3 (GSK-3)
EP1345941A1 (en) * 2000-12-20 2003-09-24 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Cyclin-dependent kinase (cdk) and glycolene synthase kinase-3 (gsk-3) inhibitors
FR2818642B1 (en) * 2000-12-26 2005-07-15 Hoechst Marion Roussel Inc NOVEL DERIVATIVES OF PURINE, PROCESS FOR PREPARING THEM, THEIR USE AS MEDICAMENTS, PHARMACEUTICAL COMPOSITIONS AND THEIR NEW USE
US7605175B2 (en) 2001-03-02 2009-10-20 Gpc Biotech Ag Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
US6812232B2 (en) 2001-09-11 2004-11-02 Amr Technology, Inc. Heterocycle substituted purine derivatives as potent antiproliferative agents
US6667311B2 (en) * 2001-09-11 2003-12-23 Albany Molecular Research, Inc. Nitrogen substituted biaryl purine derivatives as potent antiproliferative agents
JP2005512972A (en) * 2001-10-12 2005-05-12 アイアールエム エルエルシー Kinase inhibitor scaffolds and methods for their preparation
ATE355291T1 (en) 2001-12-18 2006-03-15 Cv Therapeutics Inc A2A ADENOSINE RECEPTOR ANTAGONISTS
KR20040097126A (en) * 2002-02-15 2004-11-17 씨브이 쎄러퓨틱스, 인코포레이티드 Polymer coating for medical devices
EA007272B1 (en) 2002-03-13 2006-08-25 Янссен Фармацевтика Н. В. New inhibitors of histone deacetylase
US7767679B2 (en) 2002-03-13 2010-08-03 Janssen Pharmaceutica N.V. Sulfonylamino-derivatives as novel inhibitors of histone deacetylase
GB0219052D0 (en) * 2002-08-15 2002-09-25 Cyclacel Ltd New puring derivatives
GB0219054D0 (en) 2002-08-15 2002-09-25 Cyclacel Ltd New purine derivatives
GB0219746D0 (en) * 2002-08-23 2002-10-02 Inst Of Ex Botany Ascr Azapurine derivatives
EP1556129A4 (en) * 2002-10-15 2011-02-09 Irm Llc Compositions and methods for inducing osteogenesis
AU2004230867B2 (en) 2003-04-07 2010-09-09 Agennix Usa Inc. Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
KR100573861B1 (en) * 2003-07-18 2006-04-25 경동제약 주식회사 Preparing Methods for 2-Amino-9-2-halogenoethylpurine and 2-Amino-6,8-dichloro-9-2-hydroxyethylpurine as an Intermediate thereof
CN100447143C (en) * 2003-08-15 2008-12-31 Irm责任有限公司 Compounds and compositions as inhibitors of receptor tyrosine kinase activity
AU2004264419B2 (en) * 2003-08-15 2009-01-15 Irm Llc 6-substituted anilino purines as RTK inhibitors
AP2006003517A0 (en) * 2003-09-25 2006-02-28 Janssen Pharmaceutica Nv Hiv replication purine derivatives.
AU2004309415B2 (en) 2003-12-23 2010-08-26 Agennix Usa Inc. Inhibitors of cyclin-dependent kinases, compositions and uses related thereto
JP2006056879A (en) * 2004-07-21 2006-03-02 Kobe Univ Insulin resistance-improving agent and method for screening the same
EP1781639B1 (en) 2004-07-28 2012-01-25 Janssen Pharmaceutica NV Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase
GB0419175D0 (en) * 2004-08-27 2004-09-29 Cyclacel Ltd Method of treatment and compositions
PL1799230T3 (en) * 2004-08-27 2013-05-31 Cyclacel Ltd Purine and pyrimidine cdk inhibitors and their use for the treatment of autoimmune diseases
ES2308551T3 (en) 2004-10-13 2008-12-01 F. Hoffmann-La Roche Ag PIRAZOLOBENZODIAZEPINAS DISUSTITUIDES USEFUL AS INHIBITORS FOR CDK2 AND ANGIOGENESIS, AND FOR THE TREATMENT OF CANCER OF MAMA, COLON, PULMON AND PROSTATE.
EP1837033A4 (en) * 2004-11-12 2010-05-26 Kazuhito Tomizawa REMEDY FOR DIABETES CONTAINING Cdk5 INHIBITOR
KR100677396B1 (en) * 2004-11-20 2007-02-02 엘지전자 주식회사 A method and a apparatus of detecting voice area on voice recognition device
EP1881987B1 (en) * 2005-05-16 2016-10-19 Prometic Pharma Smt Limited Purine derivatives and their use for treatment of autoimmune diseases
US8071609B2 (en) 2005-08-11 2011-12-06 Ariad Pharmaceuticals, Inc. Unsaturated heterocyclic derivatives
CA2628227A1 (en) * 2005-11-22 2007-05-31 The Scripps Research Institute Chemical synthesis of a highly potent epothilone
CN101370790B (en) 2006-01-19 2015-10-21 詹森药业有限公司 As pyridine and the pyrimidine derivatives of NSC 630176
WO2007085188A1 (en) 2006-01-27 2007-08-02 Shanghai Hengrui Pharmaceutical Co. Ltd. Pyrrolo [3,2-c] pyridine-4-one 2-indolinone protein kinase inhibitors
GB0606283D0 (en) * 2006-03-29 2006-05-10 Cyclacel Ltd Process
JP5486928B2 (en) * 2007-02-26 2014-05-07 ヴァイティー ファーマシューティカルズ，インコーポレイテッド Cyclic urea and carbamate inhibitors of 11β-hydroxysteroid dehydrogenase 1
GB0706632D0 (en) * 2007-04-04 2007-05-16 Cyclacel Ltd New purine derivatives
WO2008135232A1 (en) * 2007-05-02 2008-11-13 Riccardo Cortese Use and compositions of purine derivatives for the treatment of proliferative disorders
UA99459C2 (en) * 2007-05-04 2012-08-27 Астразенека Аб 9-(pyrazol-3-yl)- 9h-purine-2-amine and 3-(pyraz0l-3-yl)-3h-imidazo[4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer
WO2008138184A1 (en) 2007-05-14 2008-11-20 Shanghai Hengrui Pharmaceutical Co.Ltd. Derivatives of pyrroloazacycles, the method of making them and the use thereof as inhibitors of protein kinases
WO2008138232A1 (en) 2007-05-14 2008-11-20 Shanghai Hengrui Pharmaceutical Co., Ltd. Pyrrolo-nitrogenous heterocyclic derivatives, the preparation and the pharmaceutical use thereof
JP5451611B2 (en) * 2007-07-26 2014-03-26 ヴァイティー ファーマシューティカルズ，インコーポレイテッド Cyclic inhibitor of 11β-hydroxysteroid dehydrogenase 1
FR2920776B1 (en) * 2007-09-12 2012-09-28 Centre Nat Rech Scient USE OF PURINE DERIVATIVES FOR THE MANUFACTURE OF A MEDICINAL PRODUCT
JP5638955B2 (en) * 2007-10-26 2014-12-10 エフ．ホフマン−ラ ロシュ アーゲーＦ． Ｈｏｆｆｍａｎｎ−Ｌａ Ｒｏｃｈｅ Ａｋｔｉｅｎｇｅｓｅｌｌｓｃｈａｆｔ Purine derivatives useful as PI3 kinase inhibitors
AR069207A1 (en) * 2007-11-07 2010-01-06 Vitae Pharmaceuticals Inc CYCLIC UREAS AS INHIBITORS OF THE 11 BETA - HIDROXI-ESTEROIDE DESHIDROGENASA 1
WO2009075835A1 (en) 2007-12-11 2009-06-18 Vitae Pharmaceutical, Inc CYCLIC UREA INHIBITORS OF 11β-HYDROXYSTEROID DEHYDROGENASE 1
TW200934490A (en) * 2008-01-07 2009-08-16 Vitae Pharmaceuticals Inc Lactam inhibitors of 11 &abgr;-hydroxysteroid dehydrogenase 1
JP5490020B2 (en) * 2008-01-24 2014-05-14 ヴァイティー ファーマシューティカルズ，インコーポレイテッド Cyclic carbazate and semicarbazide inhibitors of 11β-hydroxysteroid dehydrogenase 1
JP5734666B2 (en) * 2008-02-11 2015-06-17 ヴァイティー ファーマシューティカルズ，インコーポレイテッド 1,3-oxaazepan-2-one and 1,3-diazepan-2-one inhibitors of 11β-hydroxysteroid dehydrogenase 1
US8598160B2 (en) * 2008-02-15 2013-12-03 Vitae Pharmaceuticals, Inc. Cycloalkyl lactame derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1
US20110105504A1 (en) * 2008-03-18 2011-05-05 Vitae Pharmaceuticals ,Inc. Inhibitors Of 11beta-Hydroxysteroid Dehydrogenase Type 1
US8242111B2 (en) * 2008-05-01 2012-08-14 Vitae Pharmaceuticals, Inc. Cyclic inhibitors of 11β-hydroxysteroid dehydrogenase 1
PL2300461T3 (en) * 2008-05-01 2013-09-30 Vitae Pharmaceuticals Inc Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1
CL2009001058A1 (en) 2008-05-01 2010-09-10 Vitae Pharmaceuticals Inc Compounds derived from substituted oxazines, inhibitors of 11b-hydroxysteroid dehydrogenase type-1; pharmaceutical composition; and use of the compound to inhibit the activity of 11b-hsd1, as in the treatment of diabetes, dyslipidemia, hypertension, obesity, cancer, glaucoma, among others.
JP5538365B2 (en) 2008-05-01 2014-07-02 ヴァイティー ファーマシューティカルズ，インコーポレイテッド Cyclic inhibitor of 11β-hydroxysteroid dehydrogenase 1
WO2009146406A1 (en) * 2008-05-30 2009-12-03 Genentech, Inc. Purine pi3k inhibitor compounds and methods of use
KR20110036602A (en) 2008-07-03 2011-04-07 서트리스 파마슈티컬즈, 인코포레이티드 Benzimidazoles and related analogs as sirtuin modulators
CA2729998A1 (en) 2008-07-25 2010-01-28 Boehringer Ingelheim International Gmbh Inhibitors of 11beta-hydroxysteroid dehydrogenase 1
EP2687525B1 (en) 2008-07-25 2015-09-23 Boehringer Ingelheim International GmbH Cyclic inhibitors of 11-beta-hydroxysteroid dehydrogenase 1
WO2010056311A1 (en) 2008-11-12 2010-05-20 Ariad Pharmaceuticals, Inc. Pyrazinopyrazines and derivatives as kinase inhibitors
CZ302122B6 (en) * 2009-01-28 2010-10-20 Univerzita Palackého v Olomouci Substituted derivatives of 6-(2-aminobenzylamino)purine, their use as well as a medicament and compositions in which said derivatives are comprised
WO2010089303A1 (en) 2009-02-04 2010-08-12 Boehringer Ingelheim International Gmbh CYCLIC INHIBITORS OF 11 β-HYDROXYSTEROID DEHYDROGENASE 1
WO2010093808A1 (en) 2009-02-11 2010-08-19 Reaction Biology Corp. Selective kinase inhibitors
WO2010103473A1 (en) * 2009-03-10 2010-09-16 Chu De Brest Method of treatment of polycystic diseases and chronic lymphocytic leukemia
ES2500643T3 (en) * 2009-04-03 2014-09-30 Verastem, Inc. Purine compounds substituted with pyrimidine as kinase inhibitors
TW201039034A (en) * 2009-04-27 2010-11-01 Chunghwa Picture Tubes Ltd Pixel structure and the method of forming the same
UA109255C2 (en) 2009-04-30 2015-08-10 Берінгер Інгельхайм Інтернешнл Гмбх Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1
GEP20156309B (en) * 2009-04-30 2015-07-10 Vitae Pharmaceuticals Inc Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1
US8927539B2 (en) 2009-06-11 2015-01-06 Vitae Pharmaceuticals, Inc. Cyclic inhibitors of 11β-hydroxysteroid dehydrogenase 1 based on the 1,3-oxazinan-2-one structure
SI2448938T1 (en) 2009-06-29 2014-08-29 Incyte Corporation Experimental Station Pyrimidinones as pi3k inhibitors
EP2448928B1 (en) 2009-07-01 2014-08-13 Vitae Pharmaceuticals, Inc. Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1
TW201130842A (en) * 2009-12-18 2011-09-16 Incyte Corp Substituted fused aryl and heteroaryl derivatives as PI3K inhibitors
WO2011075643A1 (en) * 2009-12-18 2011-06-23 Incyte Corporation Substituted heteroaryl fused derivatives as pi3k inhibitors
US9180127B2 (en) 2009-12-29 2015-11-10 Dana-Farber Cancer Institute, Inc. Type II Raf kinase inhibitors
WO2011106168A1 (en) * 2010-02-24 2011-09-01 Dcam Pharma Inc Purine compounds for treating autoimmune and demyelinating diseases
US9193721B2 (en) 2010-04-14 2015-11-24 Incyte Holdings Corporation Fused derivatives as PI3Kδ inhibitors
WO2011159726A2 (en) 2010-06-14 2011-12-22 The Scripps Research Institute Reprogramming of cells to a new fate
JP5860042B2 (en) 2010-06-16 2016-02-16 ヴァイティー ファーマシューティカルズ，インコーポレイテッド Substituted 5, 6 and 7 membered heterocycles, medicaments containing such compounds and their use
US9062055B2 (en) 2010-06-21 2015-06-23 Incyte Corporation Fused pyrrole derivatives as PI3K inhibitors
WO2011161128A1 (en) 2010-06-25 2011-12-29 Boehringer Ingelheim International Gmbh Azaspirohexanones as inhibitors of 11-beta-hsd1 for the treatment of metabolic disorders
JP5555378B2 (en) 2010-07-14 2014-07-23 エフ．ホフマン−ラ ロシュ アーゲー Purine compounds selective for PI3KP110 delta and methods of use thereof
US8969556B2 (en) * 2010-10-12 2015-03-03 Case Western Reserve University Purine-based triazoles
WO2012059416A1 (en) 2010-11-02 2012-05-10 Boehringer Ingelheim International Gmbh Pharmaceutical combinations for the treatment of metabolic disorders
SG190890A1 (en) 2010-12-16 2013-07-31 Hoffmann La Roche Tricyclic pi3k inhibitor compounds and methods of use
ES2764848T3 (en) 2010-12-20 2020-06-04 Incyte Holdings Corp N- (1- (substituted phenyl) ethyl) -9H-purine-6-amines as PI3K inhibitors
US9108984B2 (en) 2011-03-14 2015-08-18 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
WO2012135009A1 (en) 2011-03-25 2012-10-04 Incyte Corporation Pyrimidine-4,6-diamine derivatives as pi3k inhibitors
HUE030869T2 (en) 2011-09-02 2017-06-28 Incyte Holdings Corp Heterocyclylamines as pi3k inhibitors
EP2758402B9 (en) * 2011-09-22 2016-09-14 Pfizer Inc Pyrrolopyrimidine and purine derivatives
JP6106685B2 (en) 2011-11-17 2017-04-05 ダナ−ファーバー キャンサー インスティテュート， インコーポレイテッド Inhibitors of C-JUN-N-terminal kinase (JNK)
WO2013113762A1 (en) 2012-01-31 2013-08-08 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and kits for predicting the risk of having a cutaneous melanoma in a subject
AR090548A1 (en) 2012-04-02 2014-11-19 Incyte Corp BICYCLIC AZAHETEROCICLOBENCILAMINS AS PI3K INHIBITORS
EP2664619B1 (en) * 2012-05-16 2017-07-12 Manros Therapeutics Purine derivatives as tools for screening anti-Alzheimer compounds
FR3011240A1 (en) * 2013-10-01 2015-04-03 Centre Nat Rech Scient 5'-NUCLEOTIDASE INHIBITORS AND THERAPEUTIC USES THEREOF
WO2015058140A1 (en) 2013-10-18 2015-04-23 Dana-Farber Cancer Institute, Inc. Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7)
UA115388C2 (en) 2013-11-21 2017-10-25 Пфайзер Інк. 2,6-substituted purine derivatives and their use in the treatment of proliferative disorders
CN104086551B (en) * 2014-06-06 2016-09-21 人福医药集团股份公司 Compound and its production and use
WO2015191677A1 (en) 2014-06-11 2015-12-17 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors
US10870651B2 (en) 2014-12-23 2020-12-22 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
TWI748941B (en) 2015-02-27 2021-12-11 美商英塞特公司 Salts and processes of preparing a pi3k inhibitor
JP6861166B2 (en) * 2015-03-27 2021-04-21 ダナ−ファーバー キャンサー インスティテュート， インコーポレイテッド Inhibitor of cyclin-dependent kinase
WO2016183060A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
WO2016183063A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Crystalline forms of a pi3k inhibitor
WO2017044858A2 (en) 2015-09-09 2017-03-16 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinases
WO2017091681A1 (en) 2015-11-24 2017-06-01 Aclaris Therapeutics, Inc. Selective kinase inhibitors
EP3388432A1 (en) 2017-04-10 2018-10-17 Commissariat à l'Energie Atomique et aux Energies Alternatives Purine derivatives for use as medicament and for use in treating neurodegenerative or neuro-inflammatory disorders
WO2023140640A1 (en) * 2022-01-21 2023-07-27 한양대학교 산학협력단 Heteroaryl derivative and uses thereof
CN117659016A (en) * 2022-08-26 2024-03-08 嘉兴优博生物技术有限公司 Cyclin modulators

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4028353A (en) * 1971-07-29 1977-06-07 Polaroid Corporation Novel chemical compounds
US4028358A (en) * 1973-09-04 1977-06-07 Liotta Charles L 6-Fluoro-9-perfluorobutyl purine
US4405781A (en) * 1981-03-02 1983-09-20 Polaroid Corporation Method for preparing salts of 6-chloropurine
DK167878B1 (en) * 1985-04-19 1993-12-27 Sankyo Co PIGEOLIC ACID DERIVATIVES
GB9204015D0 (en) * 1992-02-25 1992-04-08 Wellcome Found Therapeutic nucleosides
FR2699176B1 (en) * 1992-12-11 1995-03-03 Adir New bicyclic pyrimidine compounds, process for their preparation and pharmaceutical compositions containing them.
JP4004066B2 (en) * 1995-11-01 2007-11-07 ノバルティス アクチエンゲゼルシャフト Purine derivatives and process for producing the same
PL321296A1 (en) * 1995-11-14 1997-12-08 Pharmacia & Upjohn Spa Derivatives of aryl and heteroaryl purine
FR2741881B1 (en) * 1995-12-01 1999-07-30 Centre Nat Rech Scient NOVEL PURINE DERIVATIVES HAVING IN PARTICULAR ANTI-PROLIFERATIVE PRORIETES AND THEIR BIOLOGICAL APPLICATIONS

Also Published As

Publication number Publication date
NZ334061A (en) 2000-08-25
CZ33899A3 (en) 2000-03-15
EP1021186B1 (en) 2005-06-29
CN1231611A (en) 1999-10-13
CN1161356C (en) 2004-08-11
IL128323A0 (en) 2000-01-31
CZ299381B6 (en) 2008-07-09
GEP20022786B (en) 2002-09-25
SI1021186T1 (en) 2005-12-31
DE69733674D1 (en) 2005-08-04
HUP9902414A3 (en) 2002-04-29
NO323775B1 (en) 2007-07-02
KR20000029781A (en) 2000-05-25
AU731778B2 (en) 2001-04-05
TR199900683T2 (en) 2002-01-21
US5866702A (en) 1999-02-02
ES2242981T3 (en) 2005-11-16
AU3900097A (en) 1998-02-25
PL331408A1 (en) 1999-07-19
UA71890C2 (en) 2005-01-17
EP1021186A1 (en) 2000-07-26
BR9710801A (en) 2001-11-27
EP1021186A4 (en) 2000-07-26
NO990466D0 (en) 1999-02-01
WO1998005335A1 (en) 1998-02-12
PL189775B1 (en) 2005-09-30
HUP9902414A2 (en) 2001-04-28
PT1021186E (en) 2005-11-30
DK1021186T3 (en) 2005-10-17
CA2262454A1 (en) 1998-02-12
IL128323A (en) 2001-11-25
CA2262454C (en) 2006-02-07
JP2000515550A (en) 2000-11-21
DE69733674T2 (en) 2006-05-04
KR100403336B1 (en) 2003-10-30
ATE298572T1 (en) 2005-07-15
RU2220968C2 (en) 2004-01-10
NO990466L (en) 1999-03-25

Similar Documents

Publication Publication Date Title
HK1020884A1 (en) Purine inhibitors of cyclin dependent kinase 2 andikb-alpha.
NZ513402A (en) Novel nucleosides and oligonucleotide analogues
TR200102714T2 (en) Purine inhibitors of cyclin dependent kinase 2 and IkB - &amp;
ATE92749T1 (en) HAIR PERMANENT FORM REDUCING COMPOSITION CONTAINING AN AMINOMERCAPTOALKYLAMIDE OR ONE OF ITS SALTS AS A REDUCING AGENT AND ITS USE IN A HAIR PERMANENT FORM FORMING METHOD.
AU6626698A (en) Glycerolipid compounds useful for the transfer of an active substance into a target cell
AU8680291A (en) An aminoglycoside composition having substantially reduced nephrotoxicity induced by the amino glycoside
GR3036173T3 (en) Purified form of streptogramines, preparation of same and pharmaceutical compositions containing same
ZA844968B (en) 2-piperazino-pteridines
ES2013664A6 (en) 6-substituted acyclicpyrimidine nucleoside derivatives and antiviral agents containing same as active ingredients.
DE69801594D1 (en) COSMETIC COMPOSITION CONTAINING AN INDIGOTYPE CONNECTION
AU3135889A (en) Benzophenone derivatives
CS548483A2 (en) Zpusob vyroby muramylpeptidu
GR3003738T3 (en)
WO1999035912A8 (en) Tuberculocidal disinfectant
AU644085B2 (en) Antiherpes pentapeptides
DE3561948D1 (en) Oximinophosphoric acid derivatives, process for their preparation and their use as pesticides
WO1999050252A3 (en) Barbituric acid derivative and preventive and therapeutic agent for bone and cartilage containing the same
DE3665587D1 (en) Oximino phosphoric-acid derivatives, process for their preparation and their use as pesticides
DE3275083D1 (en) Cycloaliphatic alcohols

Legal Events

Date Code Title Description
PC Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee)

Effective date: 20100801